Canonical Allele Identifier: CA346062997
Gene: ADCY3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24823328T>G , CM000664.2:g.24823328T>G GRCh38
NC_000002.11:g.25046197T>G , CM000664.1:g.25046197T>G GRCh37
NC_000002.10:g.24899701T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.2767A>C ENSP00000384484.2:p.Ile923Leu
ENST00000679454.1:c.2764A>C MANE Select ENSP00000505261.1:p.Ile922Leu
ENST00000260600.9:c.2764A>C ENSP00000260600.5:p.Ile922Leu
ENST00000405392.5:c.2767A>C ENSP00000384484.2:p.Ile923Leu
ENST00000485887.1:n.36A>C
ENST00000606682.5:c.1705A>C ENSP00000475652.1:p.Ile569Leu
NM_004036.3:c.2764A>C NP_004027.2:p.Ile922Leu
XM_005264104.1:c.2767A>C XP_005264161.1:p.Ile923Leu
XM_005264105.1:c.2764A>C XP_005264162.1:p.Ile922Leu
XM_006711925.1:c.2833A>C XP_006711988.1:p.Ile945Leu
XM_011532489.1:c.2890A>C XP_011530791.1:p.Ile964Leu
XM_011532490.1:c.2887A>C XP_011530792.1:p.Ile963Leu
XM_011532491.1:c.2824A>C XP_011530793.1:p.Ile942Leu
XM_011532492.1:c.2890A>C XP_011530794.1:p.Ile964Leu
XM_011532493.1:c.2752A>C XP_011530795.1:p.Ile918Leu
XM_011532494.1:c.2692A>C XP_011530796.1:p.Ile898Leu
XM_011532495.1:c.2224A>C XP_011530797.1:p.Ile742Leu
XM_011532496.1:c.2167A>C XP_011530798.1:p.Ile723Leu
NM_001320613.1:c.2767A>C NP_001307542.1:p.Ile923Leu
NM_004036.4:c.2764A>C NP_004027.2:p.Ile922Leu
XM_011532492.2:c.2890A>C XP_011530794.1:p.Ile964Leu
XM_017003186.1:c.2830A>C XP_016858675.1:p.Ile944Leu
XM_017003187.1:c.2821A>C XP_016858676.1:p.Ile941Leu
XM_017003188.1:c.2887A>C XP_016858677.1:p.Ile963Leu
XM_017003189.1:c.2749A>C XP_016858678.1:p.Ile917Leu
XM_017003190.1:c.2626A>C XP_016858679.1:p.Ile876Leu
XM_017003191.1:c.2254A>C XP_016858680.1:p.Ile752Leu
XM_017003192.1:c.2044A>C XP_016858681.1:p.Ile682Leu
XM_017003193.1:c.2041A>C XP_016858682.1:p.Ile681Leu
NM_001320613.2:c.2767A>C NP_001307542.1:p.Ile923Leu
NM_001377128.1:c.2830A>C NP_001364057.1:p.Ile944Leu
NM_001377129.1:c.2626A>C NP_001364058.1:p.Ile876Leu
NM_001377130.1:c.2332-698A>C NP_001364059.1:n.2332-698A>C
NM_001377131.1:c.2041A>C NP_001364060.1:p.Ile681Leu
NM_001377132.1:c.2764A>C NP_001364061.1:p.Ile922Leu
NM_004036.5:c.2764A>C MANE Select NP_004027.2:p.Ile922Leu